Canonical Allele Identifier: CA10387579

Gene: MED14

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.40654533C>T , CM000685.2:g.40654533C>T	GRCh38
NC_000023.10:g.40513785C>T , CM000685.1:g.40513785C>T	GRCh37
NC_000023.9:g.40398729C>T	NCBI36
NG_016325.1:g.86020G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324817.6:c.4122G>A MANE Select	ENSP00000323720.1:p.Ser1374=
ENST00000324817.5:c.4122G>A	ENSP00000323720.1:p.Ser1374=
ENST00000416199.5:c.258G>A	ENSP00000392586.1:p.Ser86=
ENST00000433003.1:c.819G>A	ENSP00000411357.1:p.Ser273=
NM_004229.3:c.4122G>A	NP_004220.2:p.Ser1374=
XM_005272701.1:c.3774G>A	XP_005272758.1:p.Ser1258=
XM_011544000.1:c.3774G>A	XP_011542302.1:p.Ser1258=
XM_005272701.3:c.3774G>A	XP_005272758.1:p.Ser1258=
XM_011544000.3:c.3774G>A	XP_011542302.1:p.Ser1258=
XM_017029962.2:c.3774G>A	XP_016885451.1:p.Ser1258=
NM_004229.4:c.4122G>A MANE Select	NP_004220.2:p.Ser1374=